rs104886038(C;T)

Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation

Is a	genotype
of	rs104886038
Gene	DHCR7
Chromosome	11
Position	71,444,111
mentioned	by

Magnitude

3

Repute

Bad

Geno	Mag	Summary
(C;T)	3	Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
(T;T)	0	common in clinvar

see Smith-Lemli-Opitz syndrome